A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414173



Internal ID21071726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:139398728..139399490hg38UCSC Ensembl
chr5:138734417..138735179hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg38763
hg19763
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125409
Samples
Known GenesSPATA24
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414173
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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